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2,8-Dibromochrysene

Base Information Edit
  • Chemical Name:2,8-Dibromochrysene
  • CAS No.:50637-63-3
  • Molecular Formula:C18H10 Br2
  • Molecular Weight:386.085
  • Hs Code.:2903999090
  • European Community (EC) Number:256-671-7
  • UNII:D6F9GEB4P5
  • DSSTox Substance ID:DTXSID60198679
  • Nikkaji Number:J261.570C
  • Wikidata:Q72464068
  • Mol file:50637-63-3.mol
2,8-Dibromochrysene

Synonyms:2,8-Dibromochrysene;50637-63-3;EINECS 256-671-7;Chrysene, 2,8-dibromo-;erucoylchloride;D6F9GEB4P5;SCHEMBL646886;DTXSID60198679;C18-H10-Br2

Suppliers and Price of 2,8-Dibromochrysene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • 2,8-Dibromochrysene 95+%
  • 1g
  • $ 663.00
  • American Custom Chemicals Corporation
  • 2,8-DIBROMOCHRYSENE 95.00%
  • 5MG
  • $ 502.69
Total 16 raw suppliers
Chemical Property of 2,8-Dibromochrysene Edit
Chemical Property:
  • Vapor Pressure:1.17E-10mmHg at 25°C 
  • Boiling Point:526.8°C at 760 mmHg 
  • Flash Point:315.3°C 
  • PSA:0.00000 
  • Density:1.722g/cm3 
  • LogP:6.67120 
  • XLogP3:7.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:385.91288
  • Heavy Atom Count:20
  • Complexity:321
Purity/Quality:

99% *data from raw suppliers

2,8-Dibromochrysene 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C(C=CC3=C2C=CC4=C3C=CC(=C4)Br)C=C1Br
Technology Process of 2,8-Dibromochrysene

There total 17 articles about 2,8-Dibromochrysene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With nickel dichloride; In 1,2-dichloro-ethane; at 25 ℃; for 1.5h;
Guidance literature:
5-bromo-2-(6-bromo-2-naphthalenyl)benzaldehyde; With potassium tert-butylate; (methoxymethyl)triphenylphosphonium chloride; In tetrahydrofuran; at 0 - 20 ℃; for 2.5h;
With nickel dichloride; In 1,2-dichloro-ethane; at 25 ℃; for 2h;
Guidance literature:
((5-bromo-2-(6-bromo-2-naphthalenyl)phenyl)ethynyl)trimethylsilane; With potassium carbonate; In methanol; dichloromethane; at 20 ℃; for 3h;
With platinum(II) chloride; In toluene; at 85 ℃; for 8h; Reagent/catalyst; Inert atmosphere;
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